Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397509430
HBB
0.882 0.200 11 5227101 5 prime UTR variant A/- del 3
rs33981098
HBB
0.827 0.280 11 5227102 5 prime UTR variant T/C;G snv 5
rs34500389
HBB
0.851 0.280 11 5227103 5 prime UTR variant G/A;T snv 4
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs562962093
MBL2
0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs35036378
ESR2
0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 6
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 5
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 8